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Pasteur Pipette

by Shandong Chengwu Medical Products Factory 7 variants

Ref 0.5mlModel 0.2ml、0.5ml、1ml、2ml、3ml、5ml、10ml

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697390596PP01R8 Basic UDI-DI 06973905961513UDI-DIDate19 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Pasteur Pipette
Model / Reference
0.2ml、0.5ml、1ml、2ml、3ml、5ml、10ml, 0.5ml
Primary DI / UDI-DI
06973905961513
Basic UDI-DI
697390596PP01R8
EMDN Code
W05010202 Urine collection, tubes
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000003370
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shandong Chengwu Medical Products Factory

See all devices from Shandong Chengwu Medical Products Factory →

Properties

Other properties (11)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No